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EC number: 950-480-9 | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- September 2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: in accordance with guidelines
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Ascophyllum nodosum, ext.
- EC Number:
- 283-907-6
- EC Name:
- Ascophyllum nodosum, ext.
- Cas Number:
- 84775-78-0
- Molecular formula:
- Not applicable; a generic molecular formula cannot be provided for this UVCB substance.
- IUPAC Name:
- Ascophyllum nodosum, extract
- Details on test material:
- - Name of test material (as cited in study report): ALGIFERT K+
- Substance type: Dried alkaline extract of marine algae Ascophyllum nodosum dissolved in aqueous solution
- Physical state: Solid, black, micro- flakes, characteristic odour
- Analytical purity: not applicable
- Lot/batch No.: 32325-020509
- Expiry date: 02 May 2012
- Supplier: Valagro S.p.A. (sponsor)
- Storage condition of test material: the Test Article was stored in its original container, as supplied by the Sponsor at room temperature in the Test Article Stores of INTOX. The stability of the test substance in storage will be the responsibility of the Sponsor.
- pH: 9.2 (1% aqueous solution)
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Serum Institute of India Ltd., Pune; a supplier approved by the test facility management.
- Age at study initiation: Young adults (6 to 7 months)
- Weight at study initiation: 2.58 to 2.65 kg
- Housing: Animals were housed individually in stainless steel cages provided with stainless steel mesh bottom and facilities for food and water bottle.
- Diet (e.g. ad libitum): 'Amrut' brand extruded pelleted rabbit feed manufactured by Pranav Agro Ltd., Pune, provided ad libitum
- Water (e.g. ad libitum): Potable water, passed through Aqua guard water filter, and subjected to ultra violet irradiation, provided ad libitum in stainless steel bowls, throughout the acclimation and study period.
- Acclimation period: The animals were acclimated for eleven days in the experimental room before start of the experiment.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23oC
- Humidity (%): 30-70%
- Air changes (per hr): 10 - 15
- Photoperiod (hrs dark / hrs light): 12 hours light and 12 hours dark.
IN-LIFE DATES: From: 15 September 2009 To: 23 September 2009
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the untreated right eye served as a control
- Amount / concentration applied:
- 100 mg
- Duration of treatment / exposure:
- 1 hour
- Observation period (in vivo):
- 1, 24, 48, 72 hours and day 7 after the application.
- Number of animals or in vitro replicates:
- three males
- Details on study design:
- The test article ALGIFERT K+, was pulverised by using mortar and pestle before instillation in the eye of the rabbit. On test day the rabbits were fixed in rabbit-holder during application. The test article, in the amount of 100 mg, was placed in the conjunctival sac of left eye of each animal after gently pulling the lower lid away from the eyeball. Since a volume of 0.1 ml of the test article, gently compacted in a measuring cylinder, was found to weight 116 mg i.e. exceding 100 mg, the test dose was administered as 100 mg only. The eyelids were then gently held together for about one second to prevent loss of test article. The right eye remained untreated and served as the reference control. The treated and untreated eyes were washed at 1 hour following instillation with Millipore Elix- 10 system analytical grade water, to remove any residual test article.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 1 h
- Score:
- 6.7
- Max. score:
- 8
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24 hs.
- Score:
- 3.3
- Max. score:
- 4
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 48 hs.
- Score:
- 1.3
- Max. score:
- 2
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 72 hs.
- Score:
- 0.7
- Max. score:
- 2
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 7 days
- Score:
- 0
- Max. score:
- 0
- Irritant / corrosive response data:
- Maximum Group Mean Score: 6.7
Persistence of Score: Group mean total score at 48 hours >0 (as per Modified Version of the Kay and Calandra System)
Any other information on results incl. tables
SUMMARY OF OCULAR IRRITANCY SCORES
Animal ID & Sex |
Sum of Irritancy Scores at |
||||
1 |
24 |
48 |
72 |
7 |
|
h |
h |
h |
h |
Day |
|
RB7834 Male |
4 |
2 |
0 |
0 |
- |
RB7835 Male |
8 |
4 |
2 |
0 |
- |
RB7836 Male |
8 |
4 |
2 |
2 |
0 |
Group mean of the total score |
6.7 |
3.3 |
1.3 |
0.7 |
0.0 |
Maximum Group Mean Score |
6.7 |
||||
Classification as per Modified Version of the Kay and Calandra System |
|||||
Persistence of Score |
Group mean total score at 48 hours >0 |
||||
Descriptive Rating |
Mild-irritant |
Individual Animal Ocular Irritation DATA
Animal ID & Sex |
Findings |
1 |
24 |
48 |
72 |
7 |
|
|
h |
h |
h |
h |
Day |
|
|||
RB7834 Male |
Cornea |
( A ) opacity - degree of density |
0 |
0 |
0 |
0 |
- |
|
( B ) area involved |
0 |
0 |
0 |
0 |
- |
|
||
Score A x B x 5 = |
0 |
0 |
0 |
0 |
- |
|
||
Iris |
( C ) function and aspect |
0 |
0 |
0 |
0 |
- |
|
|
Score C x 5 = |
0 |
0 |
0 |
0 |
- |
|
||
Conjunctiva |
( D ) redness |
1 |
1 |
0 |
0 |
- |
|
|
( E ) chemosis |
1 |
0 |
0 |
0 |
- |
|
||
( F ) discharge |
0 |
0 |
0 |
0 |
- |
|
||
Score ( D + E + F ) x 2 = |
4 |
2 |
0 |
0 |
- |
|
||
Sum of Scores |
4 |
2 |
0 |
0 |
- |
|
||
RB7835 Male |
Cornea |
( A ) opacity - degree of density |
0 |
0 |
0 |
0 |
- |
|
( B ) area involved |
0 |
0 |
0 |
0 |
- |
|
||
Score A x B x 5 = |
0 |
0 |
0 |
0 |
- |
|
||
Iris |
( C ) function and aspect |
0 |
0 |
0 |
0 |
- |
|
|
Score C x 5 |
0 |
0 |
0 |
0 |
- |
|
||
Conjunctiva |
( D ) redness |
2 |
1 |
0 |
0 |
- |
|
|
( E ) chemosis |
2 |
1 |
0 |
0 |
- |
|
||
( F ) discharge |
0 |
0 |
0 |
0 |
- |
|
||
Score ( D + E + F ) x 2 = |
8 |
4 |
0 |
0 |
- |
|
||
Sum of Scores |
8 |
4 |
0 |
0 |
- |
|
||
RB7836 Male |
Cornea |
( A ) opacity - degree of density |
0 |
0 |
0 |
0 |
0 |
|
( B ) area involved |
0 |
0 |
0 |
0 |
0 |
|
||
Score A x B x 5 = |
0 |
0 |
0 |
0 |
0 |
|
||
Iris |
( C ) function and aspect |
0 |
0 |
0 |
0 |
0 |
|
|
Score C x 5 = |
0 |
0 |
0 |
0 |
0 |
|
||
Conjunctiva |
( D ) redness |
2 |
1 |
1 |
1 |
0 |
|
|
( E ) chemosis |
2 |
1 |
0 |
0 |
0 |
|
||
( F ) discharge |
0 |
0 |
0 |
0 |
0 |
|
||
Score ( D + E + F ) x 2 = |
8 |
4 |
2 |
2 |
0 |
|
||
Sum of Scores |
8 |
4 |
2 |
2 |
0 |
|
||
Group mean of the total score |
6.7 |
3.3 |
0.7 |
0.7 |
0.0 |
|
||
Maximum Group Mean Score |
6.7 |
|||||||
Classification as per Modified Version of the Kay and Calandra System |
||||||||
Persistence of Score |
Group mean total score at 48 hours > 0 |
|||||||
Descriptive Rating |
Mild irritant |
|||||||
Class |
4 |
INDIVIDUAL ANIMAL CLINICAL SIGNS
Animal ID. |
Time of Observation : Study Day |
||||||
1 |
2 |
3 |
4 |
5 |
6 |
7 |
|
RB7834 |
NAD |
NAD |
NAD |
NAD |
- |
- |
- |
RB7835 |
NAD |
NAD |
NAD |
NAD |
- |
- |
- |
RB7836 |
NAD |
NAD |
NAD |
NAD |
NAD |
NAD |
NAD |
Day 1 is the day of treatment. NAD – No abnormality detected,
Applicant's summary and conclusion
- Interpretation of results:
- other: mild irritant
- Remarks:
- Criteria used for interpretation of results: other: modified version of the Kay and Calandra System
- Conclusions:
- Acute eye irritation / corrosion test was performed on ALGIFERT K+ in rabbits, in compliance with the Organization for Economic Cooperation and Development (OECD) Guidelines for Testing of Chemicals, Section 4, N° 405 - Acute Eye Irritation / Corrosion, adopted on 24th April 2002.
This acute eye irritation / corrosion test, comprising of an initial test performed on one rabbit, followed by a confirmatory test on two more rabbits, revealed a maximum irritancy score of 6.7 at 1h post-application, decreasing gradually thereafter to 0 on day 7. The results indicated that the induced changes were reversible in nature, and hence were classified as ‘irritation’ and not as ‘corrosion’.
When examined in light of the criteria for evaluation, i.e. modified version of the Kay and Calandra System, based on the maximum score and persistence of the irritancy score, ALGIFERT K+ is classified as mild irritant to eye of rabbit. - Executive summary:
Testing ofALGIFERT K+for its acute irritation / corrosion potential in the rabbit eye was performed in compliance with the Organization for Economic Cooperation and Development (OECD) Guidelines for Testing of Chemicals, Section 4,N°405 - Acute Eye Irritation / Corrosion study, adopted 24th April 2002. This test was performed in accordance with the sequential testing strategy recommended in this OECD Test Guideline.Initially the test was performed using one animal. As the observations at this stage did notsuggest the test article to be severely irritating orcorrosive, the study was continued to conduct a confirmatory test involving two more animals.The test article was pulverized and an amount of 100 mg was applied as a single instillation into the lower conjunctival sac of left eye of the rabbits while the untreated right eye served as a control. Eyes were rinsed with water1 hour after application of the test article. The degree of eye irritation / corrosion was evaluated by scoring changes in conjunctiva, cornea and iris, at 1, 24, 48, 72 hours and day 7 after the application. Other effects in the eye and adverse systemic effects, if any, were observed and described. Body weights were recorded on the day of treatment and at termination of the study.The tests performed on rabbits revealed a maximum irritancy score of 6.7 at 1 h post-application, decreasing thereafter to 0 (zero) on day 7, which indicated that the induced changes were reversible in nature, and hence could be classified as ‘irritation’ and not as ‘corrosion’.The treated rabbits did not exhibit any signs of systemic toxicity throughout the period of the study. Their body weight gain was not adversely affected through the study period. When examined in light of the criteria for evaluation, i.e. modified version of the Kay and Calandra System, based on the maximum score and persistence of the irritancy score,ALGIFERT K+is classified as a mild-irritant to eye in rabbit.
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